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Dehydroformouregine
Dehydroformouregine
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Dehydroformouregine
Price:
CAS No.: 107633-69-2
Catalog No.: CFN96155
Molecular Formula: C20H19NO4
Molecular Weight: 337.4 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The herbs of Piper nigrum
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF
Similar structural: Comparison (Web)  (SDF)
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Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
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Biological Activity
Description: Standard reference
Dehydroformouregine Description
Source: The herbs of Piper nigrum
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.9638 mL 14.8192 mL 29.6384 mL 59.2768 mL 74.096 mL
5 mM 0.5928 mL 2.9638 mL 5.9277 mL 11.8554 mL 14.8192 mL
10 mM 0.2964 mL 1.4819 mL 2.9638 mL 5.9277 mL 7.4096 mL
50 mM 0.0593 mL 0.2964 mL 0.5928 mL 1.1855 mL 1.4819 mL
100 mM 0.0296 mL 0.1482 mL 0.2964 mL 0.5928 mL 0.741 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
Structure Identification:
The Alkaloids: Chemistry and Pharmacology.1989;35:1–76.
Chapter 1 Alkaloids from Guatteria.[Reference: WebLink]

METHODS AND RESULTS:
Dehydronornuciferine and O-methyldehydroisopiline are isolated from G. ouregou, where they cooccur with the corresponding noraporphines, and the N-formyl derivatives Dehydroformouregine and formouregine.
Chinese Traditional & Herbal Drugs, 2015 , 46 (21) :3146-3150.
Chemical constituents of Sabia parviflora.[Reference: WebLink]
To investigate the chemical constituents from the stems and leaves of Sabia parviflora.
METHODS AND RESULTS:
Column chromatographies over silica gel, Sephadex LH-20, reverse phase C_(18), MCI, and semi-preparative HPLC were used repeatedly for separation and purification of chemical constituents, and their structures were identified by NMR and MS spectra data with those reported in literature. Fourteen compounds were obtained from the petroleum ether extract of S. parviflora, and identified as β-sitosterol(1), mominine(2),(20S)-3-oxo-20-hydroxytaraxastane(3), fluoren-9-one(4), N-formyldehydroanonain(5), betulinic acid(6), Dehydroformouregine(7), palmitic acid(8), 20-hydroxy-lupan-3-one(9), 3-oxooleanolic acid(10), erythrodiol(11), methyl betulinate(12), N-formyl-annonain(Z)(13), and N-formyl-O-methylisopiline(14).
CONCLUSIONS:
Among the 14 compounds, there are seven pentacyclic triterpenes, four alkaloids, and three other compounds; compounds 3—10 and 12—14 are isolated from this plant and the plants of Sabia Colebr. for the first time, and the ~(13)C-NMR spectral assignments of compounds 5, 7, and 14 are reported for the first time.
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